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Myofascial Pain Syndromes clinical trials

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NCT ID: NCT01203865 Recruiting - Fibromyalgia Clinical Trials

Prevalence of Fibromyalgia in Israel

Start date: October 2010
Phase: N/A
Study type: Observational

The prevalence of fibromyalgia syndrome in the Israeli population is of importance fro planning resource allocation of medical expenditure as well as for identifying demographic and ethnic differences of this unique population compared with other western samples. In the current study the investigators aim at estimating the prevalence of fibromyalgia in this population. For this purpose a two - stage process will be used. First, a population survey will be conducted by telephone, screening for widespread pain and fatigue in the general population. This survey will use the London Fibromyalgia Epidemiology Study Screening Questionnaire. Second, a sample of patients attending the rheumatology clinic will be surveyed with this tool and will be examined in order to determine the actual proportion of patients fulfilling ACR criteria for fibromyalgia. This will enable us to calculate the positive predictive value of the London Fibromyalgia Epidemiology Study Screening Questionnaire in our population and hence to calculate the prevalence of fibromyalgia in the population.

NCT ID: NCT01189994 Recruiting - Fibromyalgia Clinical Trials

Trial of Acupuncture in the Treatment of Fibromyalgia

Start date: September 2010
Phase: N/A
Study type: Interventional

Fibromyalgia is a medical condition characterized by musculoskeletal pain, fatigue, sleep disturbances and depression. It affects population at a socioeconomically active age and represents a burden for the patients and the health care system due to its personal and functional implications. At this moment, there is no completely effective treatment for fibromyalgia, and acupuncture has been a promising alternative. This trial aims to evaluate if addition of acupuncture to standard care represents an improvement in comparison with standard care only. Thus, patients enrolled in this trial will be randomly allocated into one of two groups: group A, who besides standard treatment will receive 12 sessions of acupuncture; and group B, who will receive standard care with monthly orientation sessions for the same period. Patients will be evaluated at baseline, after completion of acupuncture treatment or orientation, and after an additional 12-week follow up. Evaluation will be based on diaries of pain and medication, and standard scales of pain, quality of life and disability.

NCT ID: NCT01180244 Completed - Fibromyalgia Clinical Trials

The Clinical Effect of Low-Intensity Electromagnetic Field Neurostimulation in Fibromyalgia Syndrome Patients

Start date: January 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether persons treated with a low-intensity, noninvasive form of cortical electrical stimulation experience a reduction in symptoms of fibromyalgia different than persons receiving a sham treatment. Outcome measures include reduction in patient pain levels and improvement in sleep measures.

NCT ID: NCT01174667 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Massage of the Low Back Muscles Assessed With Ultrasound Scanning

Start date: September 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the study is to use diagnostic ultrasound to compare the thickness of soft tissues in the low back in a group of patients with chronic low back pain treated with massage to a control group of non-treated patients. It is hypothesized that on average, soft tissue thickness in the lumbar region will change in the group receiving massage compared to the control group.

NCT ID: NCT01173055 Completed - Fibromyalgia Clinical Trials

A Study to Evaluate the Effects of Milnacipran on Pain Processing and Functional MRI in Patients With Fibromyalgia

Start date: June 2010
Phase: Phase 4
Study type: Interventional

Fibromyalgia is a condition that includes pain, tenderness, stiff muscle, and fatigue. Researchers want to find out if "a drug" called milnacipran can help people with fibromyalgia. milnacipran (Savella) is approved by the FDA for the management of fibromyalgia. In this study, milnacipran will be given to find out more about how it affects pain and thinking in people with fibromyalgia.

NCT ID: NCT01167413 Not yet recruiting - Fibromyalgia Clinical Trials

Frequency of Axial Spondyloarthropathy Among Patients Suffering From Fibromyalgia

Start date: August 2010
Phase: N/A
Study type: Observational

Fibromyalgia Syndrome (FMS) is a non - inflammatory condition characterized by the presence of chronic, widespread musculoskeletal pain and tenderness; FMS is considered to be the result of increased processing of pain by the central nervous system. Axial spondyloarthropathy is the hallmark of Ankylosing Spondylitis (AS), an inflammatory joint disease involving the axial spine, the sacroiliac joints as well as peripheral joints. Although FMS and AS differ vastly in their pathogenesis, a considerable clinical overlap may exist between these conditions. Both disorders typically cause chronic nocturnal back pain and disturbed sleep may accompany either condition. In addition,the investigators have previously described an increased prevalence of (secondary) FMS among female AS patients. This overlap may have important clinical implications since the presence of comorbid FMS may lead to increased severity results on commonly used instruments in the evaluation of disease activity in AS, such as the BASDAI and BASFI . Recently, the Assessment of Spondyloarthritis international Society (ASAS) has published updated classification criteria for axial spondyloarthropathy. These criteria, which are summarized in table 1, are based on the evaluation of patients suffering from chronic back pain with an age of onset of less than 45. Objective: The objective of the current study is to evaluate the prevalence of axial spondyloarthropathies among FMS patients, utilizing the new ASAS criteria.

NCT ID: NCT01167036 Completed - Clinical trials for Myofascial Pain Syndrome

Effectiveness of a Massage Instrument Compared to Placebo for Upper Trapezius Muscle Pain

Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study was to determine if using a specialized massage tool was more effective than a placebo treatment in relieving pain in the upper trapezius muscle along the top of the shoulder.

NCT ID: NCT01163409 Enrolling by invitation - Fibromyalgia Clinical Trials

Exercise, Acupuncture and Fibromyalgia

Start date: June 2010
Phase: N/A
Study type: Interventional

Set of real acupuncture treatment and supervised aerobic exercise have better efficacy in pediatric patients with fibromyalgia versus treatment with sham acupuncture and supervised aerobic exercise, as well as treatment versus combination with aerobic exercise and resistance exercise the major muscle groups, both supervised versus group control, who just get guidance for physical activity.

NCT ID: NCT01151163 Recruiting - Fibromyalgia Clinical Trials

Peripheral Arterial Tonometry (PAT) Evaluation of Sleep in Fibromyalgia

Start date: January 2011
Phase: N/A
Study type: Observational

Fibromyalgia syndrome (FMS) is characterized by the presence of widespread pain, chronic fatigue and typical sleep disturbances. The purpose of the current study is to investigate the nature of sleep disturbance in FMS, using a novel technology. Peripheral arterial tonometry is a method by which peripheral arterial tone is measured non - invasively using in an ambulatory setup during sleep. The information collected reflects autonomic nervous system function and respiratory changes during sleep. We intend to utilize this technique in order to improve our understanding of the interrupted patterns of sleep in FMS and as a possible biomarker which may be used in the future to follow up FMS patients and their response to treatment.

NCT ID: NCT01149018 Recruiting - Fibromyalgia Clinical Trials

Efficacy Trial of Oral Tetrahydrocannabinol in Patients With Fibromyalgia

Start date: June 2010
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate the effectiveness of oral tetrahydrocannabinol in patients suffering from Fibromyalgia